Quantifying Biochemical Communication in Hepatocellular Carcinoma
量化肝细胞癌的生化通讯
基本信息
- 批准号:9566890
- 负责人:
- 金额:$ 14.33万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:AlkylationAmino AcidsAmino Acyl-tRNA SynthetasesAnimalsBiochemicalBiologicalBiosensorCancer EtiologyCell LineCellsCessation of lifeClinicCommunicationComplementComplexCyclic AMP-Dependent Protein KinasesCysteineDataData SetDevelopmentDiagnosisDiagnosticDiseaseDisease ProgressionDistant MetastasisDrug TargetingEngineeringFluorescenceGoalsGray unit of radiation doseGrowthHydroxyl RadicalInflammatoryLeadLeftLinkLiteratureMAPK14 geneMammalian CellMeasurementMembraneMetabolicMetabolic PathwayMetastatic toModelingMolecular ProbesMonitorMutagenesisNatureNebraskaNeoplasm MetastasisObesityPeptidesPhenotypePhospho-Specific AntibodiesPhosphorylationPhosphorylation SitePhosphotransferasesPrevalencePrimary carcinoma of the liver cellsProductionProtein IsoformsProtein KinasePublic HealthRNARattusResearchSamplingSeveritiesSignal PathwaySignal TransductionSurvival RateTherapeutic InterventionTimeTissuesUnited StatesWorkanalogbasecell motilitychelationclinical developmentclinical diagnosticsfluorophorehepatocellular carcinoma cell linehuman tissueinterdisciplinary approachinterestnew therapeutic targetnon-alcoholic fatty liver diseasenovelnovel diagnosticsprogramssensorstatisticstherapeutic targettrendtumorunnatural amino acids
项目摘要
ABSTRACT
Rates of hepatocellular carcinoma (HCC) have been steadily increasing in the United States. One explanation
for this observation is the alarming trend in obesity. A positive correlation between the development of non-
alcoholic fatty liver disease (NAFLD) and HCC has been identified in the clinic, supporting a link between
obesity and HCC. The public health impact of HCC is further exacerbated by the difficulty in detecting HCC
tumors in the clinic, leading to the majority of tumors identified in the clinic presenting with preexisting
metastasis. The aggressive nature of the disease at diagnosis results in a dismal five-year survival rate of 15
percent. The long-term goal of the proposed work is to delineate the longitudinal signaling perturbations that
lead to NAFLD and subsequent progression to metastatic HCC. This project will: 1) develop a signaling profile
of NAFLD, 2) delineate signaling changes associated with progression of HCC to a metastatic phenotype, and
3) investigate spatially localized signaling in metastatic HCC. As a central component of this work, a panel of
direct protein kinase activity sensors will be employed for inflammatory, growth, survival, cell motility, and
metabolic pathways. This panel of novel kinase activity sensors relies on the incorporation of a
phosphorylation-sensitive amino acid into kinase-selective substrates, allowing for a direct fluorescence-based
readout of kinase enzymatic activity in complex biological samples. To complement this initiative, this project
will leverage a multidisciplinary approach to correlate observed changes in kinase signaling with changes in
RNA and metabolite production. This multipronged approach will permit the identification of regulators, as well
as effectors, of altered kinase activity observed in the disease state. Taken together, the proposed project will
provide a quantitative picture of signaling perturbations in NAFLD, establish correlations between kinase
activity and invasive phenotypes in HCC, and enable the analysis of spatially restricted kinase activity in HCC
cell lines. In the long-term, this work will provide a basis for the development of clinical diagnostics and identify
potential new targets for therapeutic intervention in the development and progression of HCC.
摘要
在美国,肝细胞癌(HCC)的发病率一直在稳步上升。一种解释
因为这是肥胖的惊人趋势。发展与非发展之间存在正相关关系,
酒精性脂肪肝(NAFLD)和肝细胞癌已被确定在临床上,支持之间的联系,
肥胖和HCC。HCC的公共卫生影响因HCC检测的困难而进一步加剧
肿瘤在临床上,导致大多数在临床上确定的肿瘤表现为既存
转移诊断时疾病的侵袭性导致5年生存率为15
百分之这项工作的长期目标是描绘纵向信号扰动,
导致NAFLD和随后进展为转移性HCC。该项目将:1)开发信号配置文件
2)描绘与HCC进展为转移表型相关的信号传导变化,和
3)研究转移性HCC中的空间定位信号传导。作为这项工作的核心组成部分,
直接的蛋白激酶活性传感器将用于炎症、生长、存活、细胞运动,
代谢途径这一组新型激酶活性传感器依赖于掺入一种
将磷酸化敏感的氨基酸转化为激酶选择性底物,允许基于直接荧光的
复杂生物样品中激酶酶活性的读出。为配合这一举措,该项目
将利用多学科方法将观察到的激酶信号传导的变化与
RNA和代谢产物。这种多管齐下的方法也将有助于确定监管机构
作为在疾病状态中观察到的改变的激酶活性的效应物。综合而言,拟议项目将
提供NAFLD中信号扰动的定量图像,建立激酶之间的相关性,
活性和侵袭性表型,并能够分析HCC中的空间限制性激酶活性
细胞系从长远来看,这项工作将为临床诊断的发展提供基础,并确定
在HCC的发展和进展中进行治疗干预的潜在新靶点。
项目成果
期刊论文数量(0)
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{{ truncateString('Cliff I Stains', 18)}}的其他基金
Chemical Approaches for Interrogating Fundamental Biomedical Processes
用于研究基本生物医学过程的化学方法
- 批准号:
10552375 - 财政年份:2023
- 资助金额:
$ 14.33万 - 项目类别:
Chemical Approaches for Interrogating Fundamental Biomedical Processes
用于研究基本生物医学过程的化学方法
- 批准号:
10054723 - 财政年份:2016
- 资助金额:
$ 14.33万 - 项目类别:
Chemical Approaches for Interrogating Fundamental Biomedical Processes
用于研究基本生物医学过程的化学方法
- 批准号:
9142785 - 财政年份:2016
- 资助金额:
$ 14.33万 - 项目类别:
Design, Synthesis, and Application of a Real-Time MAPK Activity Sensor
实时 MAPK 活动传感器的设计、合成和应用
- 批准号:
7540713 - 财政年份:2008
- 资助金额:
$ 14.33万 - 项目类别:
Design, Synthesis, and Application of a Real-Time MAPK Activity Sensor
实时 MAPK 活动传感器的设计、合成和应用
- 批准号:
7680602 - 财政年份:2008
- 资助金额:
$ 14.33万 - 项目类别:
Design, Synthesis, and Application of a Real-Time MAPK Activity Sensor
实时 MAPK 活动传感器的设计、合成和应用
- 批准号:
7923215 - 财政年份:2008
- 资助金额:
$ 14.33万 - 项目类别:
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